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01 1Alginic Acid Alumina; Hydrated Sodium Bicarbonate
02 2Allopurinol
03 1Alumina, Hydrated; Calcium Carbonate; Sodium Alginate; Sodium Bicarbonate
04 2Amiloride Hydrochloride Dihydrate; Hydrochlorothiazide
05 1Apricot
06 1Aprotinin, Bovint
07 1Cetirizine Dihydrochloride
08 2DESMOPRESSIN ACETATE
09 3Desloratadine
10 3Dexibuprofen
11 1Docetaxel (Vattenfri)
12 1Doxycycline Hyclate
13 1Doxycycline Monohydrate
14 2Gimeracil; Oteracil Potassium; Tegafur
15 1Glucosamine Sulfate Potassium Chloride
16 1Loperamide Hydrochloride
17 1Loperamide Hydrochloride; Simethicone
18 8METHOTREXATE
19 5METHOTREXATE (METHOTREXATE SODIUM)
20 75Metadonhydroklorid
21 64Methotrexate
22 8Methotrexate Disodium
23 8Metotreksat
24 1Misoprostol
25 2My Firstborn
26 5Naloxone Hydrochloride Dihydrate; Oxycodone Hydrochloride
27 2Paracetamol
28 2Ranitidine Hydrochloride
29 1Sodium Hyaluronate
30 1Sodium Picosulfate (Monohydrate)
31 2Sodium alginate; Aluminum hydroxide; Sodium hydrogen carbonate
32 3Sodium alginate; Aluminum hydroxide; Sodium hydrogen carbonate; Calcium carbonate
33 4Tegafur; Gimeracil; Oteracilmonokalium
34 2Tegafur; Gimeracil; Oteracil
35 4Tegafur; Gimeracil; Oteracyl Potassium
36 1Terbinafinhydrochloride
37 3Xylometazoline Hydrochloride
38 4Ziprasidone Hydrochloride (Anhydrous)
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01 3Disphar International Bv
02 5NORDIC GROUP B.V.
03 8NORDIC GRP
04 2NORDIC PHARMA
05 55Nordic Drugs AB
06 55Nordic Drugs Ab
07 18Nordic Group B.V.
08 12Nordic Group BV
09 48Nordic Group Bv
10 4Nordic Pharma Bv
11 20Nordic Pharma Gmbh
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01 12Capsule
02 3Chewable Tablet
03 2Concentrate For Solution For Infusion
04 2Effervescent Tablet
05 9Film Coated Tablet
06 1Granules
07 4Hard Capsule
08 2INJECTABLE;INJECTION
09 3Inhalation Spray
10 4Injectable Solution
11 8Injectable Solution In Pre-Filled Pen
12 8Injectable Solution In Pre-Filled Syringe
13 1Oral Drops
14 25Oral Solution
15 4Oral Suspension
16 5SOLUTION
17 8SOLUTION;SUBCUTANEOUS
18 61Solution For Injection
19 2Solution For Injection/Infusion
20 50Syrup
21 16Tablet
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01 10.004MG/ML
02 10.015MG/ML
03 10.5mg/ml
04 110.0mg/0.4ml
05 110000KIE/ml
06 5100mg
07 210MG
08 110MG/0.4ML
09 110MG/0.4ML (10MG/0.4ML)
10 810mg
11 310mg/0.4ml
12 110mg/ml
13 110mg;5mg
14 3110mg
15 212.5MG
16 112.5MG/0.5ML (12.5MG/0.5ML)
17 412.5mg
18 212.5mg/0.5ml
19 3120mg
20 2125mg/0.5ml
21 3130mg
22 3140mg
23 115.0mg/0.6ml
24 4150mg
25 215MG
26 115MG/0.6ML
27 115MG/0.6ML (15MG/0.6ML)
28 215MG; 4.35MG; 11.8 MG
29 715mg
30 315mg/0.6ml
31 215mg; 4.35mg; 11.8mg
32 115mg; 435mg; 118mg
33 115mg;4.35mg;11.8mg
34 3160mg
35 217.5MG
36 117.5MG/0.7ML (17.5MG/0.7ML)
37 417.5mg
38 217.5mg/0.7ml
39 3170mg
40 2175mg/0.7ml
41 3180mg
42 3190mg
43 21mg/ml
44 12.5mg;25mg
45 120.0mg/0.8ml
46 5200mg
47 220MG
48 120MG/0.8ML
49 120MG/0.8ML (20MG/0.8ML)
50 220MG; 5.8MG; 15.8 MG
51 820mg
52 320mg/0.8ml
53 220mg/ml
54 220mg; 5.8mg; 15.8mg
55 120mg; 58mg; 158mg
56 120mg;10mg
57 120mg;5.8mg;15.8mg
58 222.5MG
59 122.5MG/ML (22.5MG/ML)
60 422.5mg
61 222.5mg/0.9ml
62 2225mg/0.9ml
63 1250mg
64 225MG
65 125MG/1ML (25MG/1ML)
66 125MG/ML
67 725mg
68 125mg/1.0ml
69 325mg/ml
70 12mg
71 130 mg;15 mg
72 3300mg
73 330mg
74 335mg
75 1400mcg
76 1400mg
77 440mg
78 140mg;20mg
79 345mg
80 2500mg
81 350mg
82 355mg
83 1595mg
84 35mg
85 15mg;2.5mg
86 15mg;50mg
87 1600mg
88 460mg
89 27.5MG
90 17.5MG/0.3ML
91 17.5MG/0.3ML (7.5MG/0.3ML)
92 47.5mg
93 27.5mg/0.3ml
94 17.5mg/ml
95 370mg
96 275mg/0.3ml
97 480mg
98 390mg
99 9Blank
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01 5Canada
02 18Estonia
03 67Norway
04 20Spain
05 90Sweden
06 20Switzerland
07 10USA
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Regulatory Info : Approved
Registration Country : Sweden
Alginic Acid Alumina; Alginic Acid Alumina; Hydrated Sodium Bicarbonate
Dosage Form : Chewable Tablet
Brand Name : Gaviscon
Dosage Strength :
Packaging :
Approval Date : 30/08/1974
Application Number : 19740830000013
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Tablet
Brand Name : Allopurinol Nordic Drugs
Dosage Strength : 100mg
Packaging :
Approval Date : 25/01/1991
Application Number : 19910125000015
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Tablet
Brand Name : Allopurinol Nordic Drugs
Dosage Strength : 300mg
Packaging :
Approval Date : 25/01/1991
Application Number : 19910125000022
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Alumina, Hydrated; Calcium Carbonate; Sodium Alginate; Sodium Bicarbonate
Dosage Form : Oral Suspension
Brand Name : Gaviscon
Dosage Strength :
Packaging :
Approval Date : 05/02/1982
Application Number : 19820205000135
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Amiloride Hydrochloride Dihydrate; Hydrochlorothiazide
Dosage Form : Tablet
Brand Name : Amyloferm
Dosage Strength : 5mg;50mg
Packaging :
Approval Date : 04/05/1990
Application Number : 19900504000149
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Amiloride Hydrochloride Dihydrate; Hydrochlorothiazide
Dosage Form : Tablet
Brand Name : Amyloferm Mite
Dosage Strength : 2.5mg;25mg
Packaging :
Approval Date : 04/05/1990
Application Number : 19900504000156
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Solution For Injection/I...
Brand Name : Trasylol
Dosage Strength :
Packaging :
Approval Date : 16/03/1977
Application Number : 38837
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection/I...
Brand Name : Trasylol
Dosage Strength : 10000KIE/ml
Packaging :
Approval Date : 13/12/1967
Application Number : 19671213000033
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Acura
Dosage Strength : 10mg
Packaging :
Approval Date : 19/04/2002
Application Number : 20020419000112
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Desloraphar
Dosage Strength : 5mg
Packaging :
Approval Date : 13/09/2012
Application Number : 20110121000033
Regulatory Info : Deregistered
Registration Country : Sweden
